EP0014106B1 - Amino-5 tétrahydro-1,2,3,4 anthraquinone et sa préparation - Google Patents

Amino-5 tétrahydro-1,2,3,4 anthraquinone et sa préparation Download PDF

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Publication number
EP0014106B1
EP0014106B1 EP80400003A EP80400003A EP0014106B1 EP 0014106 B1 EP0014106 B1 EP 0014106B1 EP 80400003 A EP80400003 A EP 80400003A EP 80400003 A EP80400003 A EP 80400003A EP 0014106 B1 EP0014106 B1 EP 0014106B1
Authority
EP
European Patent Office
Prior art keywords
anthraquinone
tetrahydro
amino
process according
preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
EP80400003A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0014106A1 (fr
Inventor
Serge Yvon Delavarenne
Bernard Dubreux
Pierre Tellier
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkema France SA
Original Assignee
Atochem SA
Elf Atochem SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Atochem SA, Elf Atochem SA filed Critical Atochem SA
Publication of EP0014106A1 publication Critical patent/EP0014106A1/fr
Application granted granted Critical
Publication of EP0014106B1 publication Critical patent/EP0014106B1/fr
Expired legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B04—CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
    • B04C—APPARATUS USING FREE VORTEX FLOW, e.g. CYCLONES
    • B04C5/00—Apparatus in which the axial direction of the vortex is reversed
    • B04C5/08—Vortex chamber constructions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/24—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
    • C07C225/26—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings
    • C07C225/32—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings of condensed quinone ring systems formed by at least three rings

Definitions

  • the present invention relates, as a new industrial product, to 5-amino-1,2,3,4-tetrahydro anthraquinone. It also relates to a process for the preparation of this compound by reduction of 5-nitro-1,2,3,4-tetrahydro anthraquinone.
  • the amino derivatives of tetrahydroanthraquinones are useful for the preparation of intermediates in the manufacture of dyes.
  • French patent application FR-A-2265724 Mitsubishi patent application FR-A-2265724 (Mitsui Taotsu)
  • the reduction according to the invention is carried out either by means of a reducing chemical compound, or by hydrogen in the presence of a catalyst.
  • the latter can be advantageously chosen from hydrogenated derivatives of anthraquinone such as tetrahydro-1,4,4a, 9a anthraquinone, hexahydro-1,2,3 , 4,4a, 9a anthracene-dione-9,10, tétrahydro-1,2,3,4 anthracènediol-9,10.
  • anthraquinone such as tetrahydro-1,4,4a, 9a anthraquinone, hexahydro-1,2,3 , 4,4a, 9a anthracene-dione-9,10, tétrahydro-1,2,3,4 anthracènediol-9,10.
  • those usually used in hydrogenation are used as catalysts. Mention may be made, for example, of those based on precious metals such as palladium or platinum, those based on nickel such as Raney nickel.
  • the reduction is carried out in the liquid phase, 5-nitro-1,2,3,4-tetrahydro anthraquinone being in solution in one of the solvents commonly used for hydrogenations.
  • solvents commonly used for hydrogenations.
  • solvents that may be mentioned are aliphatic, cycloaliphatic or aromatic hydrocarbons, ethers, tetrahydrofuran, dioxane, alcohols.
  • any solvent which does not contain a functional group which can be hydrogenated under the reaction conditions can be used.
  • the reduction can be carried out over a wide temperature range from 20 to 200 ° C. It is preferred to operate between 60 and 130 ° C. In the case of a catalytic hydrogenation, this is carried out at atmospheric pressure or under pressure. The hydrogenation is continued until the theoretical amount of hydrogen has been absorbed or until there is no longer any absorption of hydrogen.
  • Example 2 Into the autoclave of Example 1, 100 ml of ethanol, 25.7 g of 5,3-nitro-tetrahydro-1,2,3,4 anthraquinone, 0.2 g of palladium-based catalyst deposited on carbon are introduced. containing 5% palladium. The mixture is heated to 60 ° C. and hydrogen is introduced twice under a pressure of 30 bars. The absorption of hydrogen ceases after 40 minutes of reaction at 60 ° C. After separation of catalyst by filtration and concentration of the filtrate, 21.7 g of 5-amino-tetrahydro-1,2,3,4 anthraquinone are collected.
  • Example 4 The procedure is as in Example 4, replacing the amyl alcohol with the final filtrate of Example 4. After cooling, 9.8 g of a mixture of 1,2,3,4 anthraquinone tetrahydro are collected by filtration. and 5-amino-1,2,3,4-tetrahydro anthraquinone.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
EP80400003A 1979-01-19 1980-01-03 Amino-5 tétrahydro-1,2,3,4 anthraquinone et sa préparation Expired EP0014106B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR7901326 1979-01-19
FR7901326A FR2446808A1 (fr) 1979-01-19 1979-01-19 Amino-5 tetrahydro-1,2,3,4 anthraquinone et sa preparation

Publications (2)

Publication Number Publication Date
EP0014106A1 EP0014106A1 (fr) 1980-08-06
EP0014106B1 true EP0014106B1 (fr) 1983-06-08

Family

ID=9220958

Family Applications (1)

Application Number Title Priority Date Filing Date
EP80400003A Expired EP0014106B1 (fr) 1979-01-19 1980-01-03 Amino-5 tétrahydro-1,2,3,4 anthraquinone et sa préparation

Country Status (10)

Country Link
US (1) US4297288A (nl)
EP (1) EP0014106B1 (nl)
JP (1) JPS55133339A (nl)
BR (1) BR8000336A (nl)
CA (1) CA1122214A (nl)
DD (1) DD148769A5 (nl)
DE (1) DE3063637D1 (nl)
FR (1) FR2446808A1 (nl)
IN (1) IN153465B (nl)
SU (1) SU969153A3 (nl)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3787929T2 (de) * 1986-06-17 1994-03-24 Nippon Catalytic Chem Ind Verfahren zur Herstellung von 1-Aminoanthrachinon.
US4770818A (en) * 1986-10-28 1988-09-13 Ciba-Geigy Corporation Process for the preparation of 1-aminoanthraquinones

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1821035A (en) * 1927-08-18 1931-09-01 Gen Aniline Works Inc Compounds of the anthracene series and process of preparing them
DE695637C (de) * 1937-12-25 1940-08-31 I G Farbenindustrie Akt Ges Verfahren zur Herstellung von Leuko-5,6,7,8-tetrahydrochinizarin
US3966775A (en) * 1973-10-26 1976-06-29 Nippon Shokubai Kagaku Kogyo Co., Ltd. Process for the preparation of 1-substituted anthraquinones
IN143198B (nl) * 1974-04-02 1977-10-15 Mitsui Toatsu Chemicals

Also Published As

Publication number Publication date
FR2446808B1 (nl) 1982-03-12
DE3063637D1 (en) 1983-07-14
JPS55133339A (en) 1980-10-17
US4297288A (en) 1981-10-27
SU969153A3 (ru) 1982-10-23
EP0014106A1 (fr) 1980-08-06
BR8000336A (pt) 1980-10-07
CA1122214A (fr) 1982-04-20
IN153465B (nl) 1984-07-21
DD148769A5 (de) 1981-06-10
FR2446808A1 (fr) 1980-08-14

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